Projects funded by the NCN
Attempt to identify molecular basis and physiological effects of mutations in genes coding for erythrocyte membrane of patients with herditary spherocytosis
2015/19/B/NZ5/03469
Keywords:
hereditary spherocytosis red blood cell membrane mutations spectrin erythrocyte ankyrin
Descriptors:
- NZ2_2: Genomics, transcriptomics, epigenomics
- NZ5_3: Pathogenesis of human diseases
- NZ5_5: Diagnostics in human diseases
Panel:
NZ5 - Human and animal noninfectious diseases: etiology, mechanisms, diagnosis and treatment of diseases, poisonings and injuries (without neurological diseases)
Host institution :
Uniwersytet Wrocławski, Wydział Biotechnologii
woj. dolnośląskie
Principal investigator (from the host institution):
Number of co-investigators in the project: 5
Call: OPUS 10 - announced on 2015-09-15
Amount awarded: 724 944 PLN
Project start date (Y-m-d): 2016-06-20
Project end date (Y-m-d): 2021-02-19
Project duration:: 56 months (the same as in the proposal)
Project status: Project settled
Project description
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